Di-tert-butyl dicarbonate is a flammable liquid. Melting point 23 ℃, boiling point 56-57 ℃ (6.55E-2kPa).

It is used to introduce tert-butyloxycarbonyl protection group in organic synthesis. Di-tert-butyl dicarbonate (Boc anhydride) is used to introduce tert-butyloxycarbonyl protection gene in organic synthesis, especially for amino acid protection. It is widely used in the synthesis of medicine, protein and peptide synthesis, biochemical food, cosmetics and other products. Amino acid BOC reagent. It is used to introduce tert-butyloxycarbonyl (BOC) protection group in organic synthesis, especially suitable for amino acid protection. Can the hydrazine protected by tert-butyloxycarbonyl prepare fluorene methoxycarbonyl in chromogenic reagent? Esters to monitor solid aldehydes. Reagent for preparing tertiary butyloxycarbonyl protected amines. Reagent for introducing tert-butoxycarbonyl protection group. Alcohols such as tert-butoxycarbonyl derivatives can be protected by Lewis acid catalysis. Through the reaction of tert-butyloxycarbonylaminopropylene with formaldehyde, diisopropylamine and copper bromide? Reaction to prepare aminomethylpropadiene is the inactivator of many bovine plasma amine oxidase? Components of. It is used as an intermediate in medicine and organic synthesis, and is an important production method of amino-protective agent used in the synthesis of medicine and agrochemical products. Potassium tert-butanol is dissolved in anhydrous tetrahydrofuran, and dried carbon dioxide is injected at - 5~- 20 ℃ to form a slurry. It continues to maintain low temperature, and drops benzene solution to prepare di-tert-butyl tricarbonate. Dissolve it in carbon tetrachloride, add an appropriate amount of 1,4-diazabicyclo [2,2,2] octane, stir at 25 ℃ to completely release carbon dioxide, and convert it into di-tert-butyl dicarbonate.